Griffin J W, George R, Lobato C, Tyor W R, Yan L C, Glass J D
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
J Neuroimmunol. 1992 Oct;40(2-3):153-65. doi: 10.1016/0165-5728(92)90129-9.
Macrophages are important effector cells in immune-mediated demyelination. Current concepts regarding their entry and activation focus on the effects of T-cell-derived cytokines. This presentation describes the responses of macrophages and microglia to a non-inflammatory, non-immune injury, Wallerian degeneration. During Wallerian degeneration in the peripheral nervous system (PNS), macrophages are promptly and abundantly recruited from the circulation, and myelin clearance is prompt. In the central nervous system (CNS), the appearance of macrophages is markedly slower, and entry from the circulation is modest or absent. Myelin clearance is similarly delayed. The nature of the factors promoting macrophage entry and activation in Wallerian degeneration, and the bases for the differences between PNS and CNS, are relevant to current issues in immune-mediated demyelination.
巨噬细胞是免疫介导性脱髓鞘中的重要效应细胞。目前关于其进入和激活的概念集中在T细胞衍生细胞因子的作用上。本报告描述了巨噬细胞和小胶质细胞对非炎症性、非免疫性损伤——沃勒变性的反应。在周围神经系统(PNS)的沃勒变性过程中,巨噬细胞迅速且大量地从循环中募集,髓鞘清除迅速。在中枢神经系统(CNS)中,巨噬细胞的出现明显较慢,从循环中的进入较少或不存在。髓鞘清除同样延迟。促进巨噬细胞在沃勒变性中进入和激活的因素的性质,以及PNS和CNS之间差异的基础,与免疫介导性脱髓鞘的当前问题相关。